University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Treatment Centre, Addenbrooke's Hospital, Level 4, Box 289, Cambridge, CB2 0QQ, United Kingdom.
The Saban Research Institute, Developmental Neuroscience Program & Diabetes and Obesity Program, Center for Endocrinology, Diabetes and Metabolism, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA, 90027, USA; Inserm, Jean-Pierre Aubert Research Center, U1172, University Lille 2, Lille, 59045, France.
Mol Metab. 2018 Sep;15:8-19. doi: 10.1016/j.molmet.2018.04.007. Epub 2018 Apr 30.
The early life environment experienced by an individual in utero and during the neonatal period is a major factor in shaping later life disease risk-including susceptibility to develop obesity, diabetes, and cardiovascular disease. The incidence of metabolic disease is different between males and females. How the early life environment may underlie these sex differences is an area of active investigation.
The purpose of this review is to summarize our current understanding of how the early life environment influences metabolic disease risk in a sex specific manner. We also discuss the possible mechanisms responsible for mediating these sexually dimorphic effects and highlight the results of recent intervention studies in animal models.
Exposure to states of both under- and over-nutrition during early life predisposes both sexes to develop metabolic disease. Females seem particularly susceptible to develop increased adiposity and disrupted glucose homeostasis as a result of exposure to in utero undernutrition or high sugar environments, respectively. The male placenta is particularly vulnerable to damage by adverse nutritional states and this may underlie some of the metabolic phenotypes observed in adulthood. More studies investigating both sexes are needed to understand how changes to the early life environment impact differently on the long-term health of male and female individuals.
个体在子宫内和新生儿期所经历的早期生活环境是塑造后期疾病风险的主要因素,包括易患肥胖、糖尿病和心血管疾病的风险。代谢性疾病的发病率在男性和女性之间存在差异。早期生活环境如何导致这些性别差异是一个活跃的研究领域。
本综述的目的是总结我们目前对早期生活环境如何以性别特异性方式影响代谢性疾病风险的理解。我们还讨论了介导这些性别二态效应的可能机制,并强调了最近动物模型中干预研究的结果。
在生命早期经历营养不足和营养过剩的状态都会使两性易患代谢性疾病。女性似乎特别容易因宫内营养不良或高糖环境而增加脂肪堆积和葡萄糖稳态紊乱。雄性胎盘特别容易受到不良营养状态的损害,这可能是成年期观察到的一些代谢表型的基础。需要更多研究两性的研究来了解早期生活环境的变化如何对男性和女性个体的长期健康产生不同的影响。